Overview

In this role you will implement statistical analysis plans and deliver publication-ready data packages. You will collaborate with Medical Affairs biostatistics and programming teams and drive high-quality outputs within Sanofi Business Operations. You’ll develop non-routine macros, document methodologies, and ensure SOPs, timelines, and quality standards are met. You will contribute to cross-functional projects and support publication efforts through analyses and data visualization. This is an opportunity to influence medical data outputs at a global scale within a collaborative, science-driven environment.

Compensaciones / Beneficios

- hybrid work arrangement
- competitive salary range
- employee benefit programs
- equal opportunities
- global collaboration
- mentoring and professional development

Responsabilidades

- Design, develop, test, implement, and document statistical programming in SAS




- Produce publication-ready data packages (tables, listings, figures) and support post-hoc analyses
- Develop and maintain QC plans and timelines in collaboration with global teams
- Create non-routine macros and advanced programming techniques
- Collaborate with local and general biostatistics/programming teams to align outputs
- Mentor and onboard new team members and support graduate hiring as needed

Requisitos principales

- Master's degree minimum; several years of relevant experience
- Advanced SAS programming skills
- SDTM & ADaM (CDISC) and clinical data environment experience

- Stakeholder management
- Ability to manage timelines
- Independent and collaborative work style
- Advanced SAS programming
- SDTM
- ADaM (CDISC)

📌 Principal Statistical Programmer (Barcelona)
🏢 Sanofi
📍 Barcelona